Method of preparation of anticancer taxanes using 3-[(substituted-2-trialkylsilyl)ethoxycarbonyl]-5-oxazolidine carboxylic acids

ABSTRACT

This invention relates to a process for preparation of taxanes comprising  
     subjecting 7,10-diprotected intermediates 7-O-(2-haloacyl) baccatin III  6 c or 7,10-O-di-(2-haloacyl)-10-deacetylbaccatin III 6b to a step of coupling with (4S,5R)-3-[(2-alkyl/aryl-2-trialkylsilyl) ethoxy-carbonyl]-4-aryl-2-substituted-1,3-oxazolidine-5-carboxylic acid 1 in the presence of a condensation agent, an activating agent and an aromatic hydrocarbon to obtain 7-O-[2-(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3(2-unsubstituted/substituted-2-trialkylsilyl)-ethoxycarbonyl-1,3-oxazolidinyl-5-carbonyl]baccatin III 7a or 7,10-di-O[2-(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3-(2-unsubstituted/substituted-2-trialkylsilyl)ethoxy-carbonyl-1,3-oxazolidinyl-5-carbonyl]-10-deacetylbaccatin III 7b;  
     treating the coupled products 7-O-[2-(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3-(2-substituted-2-trialkylsilyl)ethoxy-carbonyl-1,3-oxazolidinyl-S-carbonyl]baccatin III 7a or 7,10-di-0-[2[(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3-(2-substituted-2-trialkylsilyl)ethoxycarbonyl-1,3-oxazolidinyl-5-carbonyl]-10-deacetylbaccatin III 7b with tetraalkylammonium halide in a haloalkane to obtain free amine of structure 8;  
     treating free amine 8 with acid chloride or acid anhydride in the presence of a base in a heterogeneous phase to obtain the intermediates of structure 9;  
     subjecting the intermediates of compound 9 to the deprotection of 2-haloacyl group under mild alkaline condition at −20 to +40° C. for 6-24 h in the presence of ammonia or aliphatic amines or aromatic amines or their combination to obtain paclitaxel or docetaxel.

[0001] The present invention relates to the process for the preparation of taxanes such as paclitaxel, docetaxel and their structural analogs using a novel oxazolidine carboxylic acid side chain.

FIELD OF THE INVENTION

[0002] The present invention relates to a novel oxazolidine carboxylic acid and a process for its preparation. The invention further relates to a process for the preparation of paclitaxel, docetaxel and their structural analogs using such oxazolidine carboxylic acid.

BACKGROUND OF THE INVENTION

[0003] Paclitaxel is a diterpene taxane found in very low concentration in the bark of Pacific yew tree Taxus brevifolia. Therefore, a number of semi-synthetic strategies have been developed for its synthesis from more readily available 10-DAB. However, the taxane nucleus is highly prone to degradation and semisynthetic crude materials are often produced contaminated with structurally similar impurities, thereby necessitating elaborate purification procedure using HPLC. In view of the above facts) it becomes highly desirable to develop alternative routes for synthesis of paclitaxel which involves minimal degradation along the synthetic pathway.

[0004] Any synthetic protocol for the semi-synthesis of paclitaxel/docetaxel generally consists of

[0005] a. selective acylation/protection at similarly reactive C-7 and C-10 hydroxyl groups. Among the 1,7,10 and 13-hydroxyl groups in 10-DAB, the order of reactivity is 7>10>13>1. Therefore, selective esterification of 13-hydroxyl group requires prior protection of both 7 and 10-hydroxyl groups. Furthermore, if acetyl group is required in the final product, as in the case of paclitaxel, then 7-hydroxyl is to be protected first followed by acetylation of 10-hydroxyl. This requires selection of appropriate protecting groups, which can be put selectively and-removed selectively under mild condition. Recently, we have explored the use of haloalkyl acid chlorides as protecting groups (U.S. Provisional Patent Application No. 60/311,077). These haloalkonoyl groups undergo hydrolysis faster than unsubstituted alkonoyl groups and their deprotection causes minimum degradation. We have found that such haloalkyl acid chlorides specifically 2-halo/2,2-dihaloalkyl acid chlorides can be used for selective protection in taxanes and can be selectively deprotected,

[0006] b. selective esterification of 13-hydroxyl group with a suitably protected N-benzoylphenylisoserine. It has been found that α-hydroxy-β-amidoaryl moiety at the 13-hydroxyl of the taxane moiety is essential for its anti-cancer activity (Wani et al J Am Chem Soc 93, pp 2325, 1971). Esterification at 13-hydroxyl of taxane is very sluggish due to its stereo-electronic disposition. It is known that the esterification step proceeds to completion with cyclic forms of α-hydroxy-β-amidoarylcarboxylic acids. Furthermore, when cyclic forms of C-13 side chain are used, no 2′-epimers are obtained as side product. Therefore, new cyclic forms of side chains, which undergo facile coupling with suitably protected 10-DAB in high yield under simple reaction condition without their use in large excess, are required for developing better and more efficient alternative routes for synthesis of paclitaxel and its analogs,

[0007] c. conversion of side chain precursor part into side chain and removal of the protecting groups from baccatin part. These reaction conditions should be mild in nature to afford final material in high yield with very few side products. For successful commercial production, it is desirable that the crude semi-synthetic taxane is produced with such purity that it could easily be purified into pharmaceutical grade material.

[0008] Most of the nitrogen protecting groups used so far in oxazolidine carboxylic acid require either harsh acidic condition or hydrogenolysis for their removal. Thus, eg. U.S. Pat. No. 5,476,954 to Bourzat et al describes an oxazolidine side chain having a tert-butoxy carbonyl protecting group on the nitrogen atom. After coupling with suitably protected 10-DAB, this protecting group is removed by treating the coupled product in an acidic medium to obtain an amine which is then converted into the corresponding benzoyl derivative. Also, Mas et al in the U.S. Pat. No. 5,616,739 describes a process in which the coupled product, obtained from coupling of an oxazolidine carboxylic acid and a protected 10-DAB, is treated in an acidic medium to achieve simultaneous removal of side chain protecting groups and 10-hydroxyl protecting group. The resultant amine is then suitably protected to obtain the taxane.

[0009] On the other hand, U.S. Pat. No. 5,637,723 issued to Rhone Poulenc Rorer S A in 1997 described an oxazolidine carboxylic acid, which incorporated benzoyl group as the nitrogen-protecting group. Consequently, the coupled product obtained from the oxazolidine carboxylic acid and protected 10-DAB, upon deprotection did not require to be protected by a benzoyl group. Again this procedure requires deprotection of the coupled product in an acidic medium.

[0010] With a view to develop side chain precursor which can be processed to paclitaxel/docetaxel after coupling with suitably protected taxane under very mild and preferably neutral condition, the applicants have

SUMMARY OF THE INVENTION

[0011] The present investigation relates to synthesis of taxanes comprising

[0012] i. subjecting 5-oxazolidine carboxylic acid of general structure 1 to the step of coupling with 7-O-(2-haloacyl)-baccatin III 6c or 7,10-O-di-(2-haloacyl)-10-deacetylbaccatin III 6b in the presence of a condensation agent and an activating agent in an aromatic hydrocarbon at a temperature between 0-100° C. to obtain 7-O-[2-(haloacyl)]-13-[(4S,5R) -4-aryl -3-(2-unsubstituted/substituted-2-trialkylsilyl)ethoxycarbonyl -1,3-oxazolidinyl-5-carbonyl]baccatin III 7a (from 6 c) and 7,10-O-di-[2-(haloacyl)]-13-[(4S,5R) -4-aryl -3-(2-unsubstituted/substituted -2-trialkylsily)ethoxycarbonyl-1,3-oxazolidinyl-5-carbonyl]-10-baccatin III 7b (from 6 b);

[0013] ii. subjecting the coupled product 7 to opening of the oxazolidine ring along with deprotection of (2-substituted-2-trialkylsilyl) ethoxycarbonyl group by treatment with a source of fluoride ions to lead to free amines 8;

[0014] iii. converting the resultant free amines 8 into the corresponding amides by known literature procedure, comprising treating the amines with acid chlorides or acid anhydrides in the presence of a base in a heterogeneous phase to obtain the intermediate 9;

[0015] iv. subjecting the intermediate 9 to selective deprotection of 2-haloacyl/2,2-dihaloacyl group under mild alkaline condition at −20 to +40° C. for 6-24 h in the presence of ammonia or aliphatic amines or aromatic amines or their combination to afford paclitaxel or docetaxel.

[0016] The complete reaction scheme is shown in Scheme I,

[0017] where

[0018] R_(a) is alkyl

[0019] found the following oxazolidine carboxylic acid of general structure 1. It has a (2-trialkylsilyl) ethoxycarbonyl/(2-alkyl/aryl-2-trialkylsilyl) ethoxycarbonyl group as nitrogen protecting group, which can be cleaved under very mild condition, and therefore degradation of taxane nucleus can be avoided. The other N,O-bifunctional protecting group then undergoes cleavage very fast without degradation under mild condition.

[0020] Therefore, these oxazolidine carboxylic acids have emerged as new type of side chain precursor for the synthesis of paclitaxel and docetaxel.

[0021] Herein, the applicants have described new intermediates for taxoid anticancer drugs, their process of synthesis and process for synthesis of paclitaxel and similar analogs using them (Scheme-I).

OBJECTS OF THE INVENTION

[0022] The object of this invention is to propose a novel oxazolidine carboxylic acid.

[0023] Another object of this invention is to propose a novel process for the preparation of anticancer taxanes.

[0024] Another object of the present invention is to propose a new process for the preparation of intermediates of taxanes.

[0025] Yet another object of this invention is to propose a process for preparation of paclitaxel, docetaxel and their analogs using intermediates, which minimise degradation during the process and thereby increase the purity of the target product.

[0026] R_(b) is selected from hydrogen, alkyl and aryl,

[0027] R_(c) and R_(d) are independently selected from hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, alkoxy, alkenyloxy, alkynloxy, aryloxy and heteroaryloxy,

[0028] R_(e) and R_(f) are independently selected from hydrogen, alkyl, alkenyl alkynyl, aryl, heteroaryl, alkoxy, alkenyloxy, alkynyloxy, aryloxy and heteroaryloxy In the preferred structure, R_(e) is hydrogen and R_(f) is aryl, more preferably p-methoxyphenyl or both R_(e) and R_(f) are methyl,

[0029] R_(g) is (substituted-2-trialkylsily)ethoxy preferably 2-(phenyl-2-trimethylsilyl)ethoxy.

DETAILED DESCRIPTION OF THE INVENTION

[0030] The present invention provides a process for the preparation of paclitaxel, docetaxel and their structural analogs. In this process (4R,5S)4-phenyl-2-substituted-3-[(2-unsubstituted/substituted -2-trialkyl-silyl)ethoxycarbonyl]-1,3-oxazolidine-5-carboxylic acids 1 is coupled with 7-O-(2-haloacyl)baccatin III 6c or 7,10-O-di(2-haloacyl)-10-deacetylbaccatin III 6b in the presence of a condensation agent and an activating agent in an aromatic hydrocarbon as solvent to obtain 7-O-[2-(haloacyl)]-13-[(4S,5R)-4-phenyl-2-substituted -3-(2-unsubstituted/substituted-2-trialkylsilyl)ethoxycarbonyl-1,3-oxazolidinyl-5-carbonyl]baccatin III or 7,10-O-di-[2-(haloacyl)]-13-[(4S, 5R)-4-phenyl-2-substituted-3-(2-unsubstituted/substituted-2-trialkylsilyl) ethoxycarbonyl-1,3-oxazolidinyl-5-carbonyl]-10-baccatin III respectively. The reaction is carried out at a temperature between 0-100° C., more preferably at 40-80° C., most preferably at 60° C. Among aromatic hydrocabrons, toluene is found most suitable.

[0031] Opening of the oxazolidine ring in the coupled product 7 along with simultaneous deprotection of the nitrogen protecting (2-trialkylsilyl)ethoxycarbonyl group was found to be structure dependent; the determining factor being the nitrogen-protecting group. In case of a (2-substituted-2-trialkylsilyl)ethoxycarbonyl group eg. (2-phenyl-2-trimethylsilyl)ethoxycarbonyl group as the nitrogen protecting group in the coupled product, the desired protection could be achieved by fluoride induced fragmentation leading to fewer side reaction. Among the sources of fluoride ion, tetraalkylammonium fluoride is preferable. The reaction is carried out by treating the coupled product 7 with two equivalents of tetraalkylammonium fluoride, preferably tetrabutylammonium fluoride in a haloalkane, preferably dichloromethane for 15-120 mins., preferably 30 mins. at 0-40° C., preferably at 25° C. to obtain the corresponding free amine 8.

[0032] Alternatively, deprotection of (2-trialkylsilyl)ethoxycarbonyl group eg. (2-trimethylsilyl)ethoxycarbonyl group or (2-substituted-2-trialkylsilyl)ethoxycarbonyl group eg. (2-phenyl-2-trimethyl-silyl)ethoxycarbonyl group, the nitrogen protecting group in the coupled product 7 can be achieved by using acidic medium. Treating coupled product 7 with 60% aqueous trifluoroacetic acid (10 times) and then mixing at a temperature between 18-25° C., preferably 22° C. for 3-6 h, preferably 4.5 hrs. effects deprotection along with desired opening of the oxazolidine ring. This is followed by usual work-up to obtain free amines 8.

[0033] The yields obtained by using acidic medium to obtain free amines 8 are more or less comparable to those obtained by using tetrabutylammonium fluoride. However, the later method provides final product eg. paclitaxel or docetaxel which are comparatively easier to purify to pharmaceutical grade material.

[0034] The free amines 8 are treated with acid chlorides or acid anhydrides in the presence of a base in a heterogeneous phase to obtain intermediates 9.

[0035] The intermediate 9, under mild alkaline condition, in the presence of ammonia or aliphatic amines or aromatic amines or their combination, preferably ammonia and pyridine (2:10) undergoes selective deprotection of 2-haloacyl groups without any appreciable degradation. The reaction is carried out at 0-5° C., preferably 2° C. under stirring for 6-24 h, preferably 10 h to obtain paclitaxel or docetaxel.

[0036] According to this invention is provided a process for the preparation of 4-phenyl-3-[(2-unsubstituted/substituted-2-trialkylsily) ethoxy-carbonyl]-2-substituted-1,3-oxazolidine-5-carboxylic acids 1 comprising

[0037] i. subjecting a haloformate such as a (2-unsubstituted/substituted-2-trialkylsily)ethyl haloformate to the step of condensation with arylisocrine 2 eg. phenylisoserine in the presence of a base such as alkali hydroxide or carbonate or bicarbonate or any other acid neutralising chemical;

[0038] ii. converting the isoserine 3 thus obtained into the corresponding ester 4 in the presence of an alcohol, preferably methanol and an activating agent such as dicyclohexylcarbodiimide or carbonyldiimidazole. The methyl ester 4 is alternatively prepared by condensing the intermediate 3 with diazomethane or treating it with alkyl halide in the presence of a base such as potassium bicarbonate in acetone;

[0039] iii. converting the isoserine ester 4 into 3-[(2-unsubstituted/substituted-2 trialkylsilyl) ethoxycarbonyl]-5-oxazolidine carboxylic ester 5 in the presence of chemicals such as alkoxyalkane or gem-dialkoxylkane or 1,1,1-trialkoxyalkane. The reaction is catalysed by p-arylsulfonic acids or their pyridinium salt;

[0040] iv. converting the 5-oxazolidine carboxylic ester 5 into the corresponding acid 1 by hydrolysis with alkali hydroxide or carbonate followed by treatment with mineral acid.

[0041] The invention will now be explained in greater details with the help of the accompanying experiments.

EXPERIMENTAL

[0042] Synthesis of 7-O-Chloroacetyl-10-deacetylbaccatin III (6a)

[0043] A mixture of 10-deacetylbaccatin III (250 gm, 0.46 mole), pyridine (150 gm) and 4-DMAP (5.6 gm, 46 mmol) is dissolved in dichloromethane (2.0L). The reaction mixture is stirred for 10 mins. Chloroacetylchloride (75 gm, 0.66 mole) dissolved in dichloromethane (1.5L) is then slowly added to the reaction mixture at 25-30° C. The whole mixture is stirred for 20 mins. and then excess reagent is decomposed by adding 100 gm ice water, and acidified with 5% hydrochloric acid. The organic layer thus obtained is successively washed with aqueous sodium bicarbonate, sodium chloride solution, dried over anhydrous sodium sulfate and then distilled under reduced pressure. The residue is dissolved in toluene (1.5L) at 70-80° C. and then cooled down to 0-5° C. The resulting fine solid is filtered and then washed with 1000 ml of hexane to obtain the pure title compound 6a (250 gm, 0.40 mole, yield 87%).

[0044] Synthesis of 7-O-chloroacetylbaccatin III (6c)

[0045] 7-O-Chloroacetyl-10-deacetylbaccatin III (250gm, 0.40 mole) is dissolved in pyridine (2.5L). The reaction mixture is cooled to 0-5° C. 190gm (2.42 mole) of acetyl chloride is slowly added to the reaction mixture at 0-5° C. over a period of 40-50 min. Then the resulting mixture is further stirred 0-5C. for 3 h. The excess reagent is decomposed by adding 200 ml water maintaining internal temperature 0-5° C. The solvent is then removed under reduced pressure and the residual mass is extracted with 2.5L of ethyl acetate. The organic layer thus obtained is washed with aqueous hydrochloric acid, sodium bicarbonate and sodium chloride solution. The organic layer is evaporated under reduced pressure. The residue is dissolved in toluene (1.5L) at 70-80° C. and then cooled down to 0° C. The resulting fine solid is filtered and then washed with 800 ml of hexane to obtain the pure title compound 6c (249.1 gm, 0.376 mole, yield 94%).

[0046] Synthesis of 7,10-di-O-chloroacetyl-10-deacetylbaccatin III (6b)

[0047] A mixture of 10-deacetylbaccatin III (250 gm, 0.46 mole), pyridine (300 gm) and DMAP (11.2 gm, 92 mmol) is dissolved in 2.0L of dichloromethane. The react mixture is stirred for 10 minutes. 150 gm (1.33 mole) of chloroacetyl chloride dissolved 1.5 L dichloromethane is slowly added to the reaction mixture at 25-30° C. Then, whole mixture is stirred for 20 minutes. 150 gm Ice water is added to decompose excess reagent, and then the reaction mixture is acidified with 5% hydrochloric acid.

organic layer thus obtained is successively washed with aqueous sodium-bicarbon

sodium chloride solution, dried over anhydrous sodium sulfate, and then distilled un

reduced pressure. The residue is dissolved in toluene (1.5 L) at 70-80° C. and then coo

down to 0-5° C. The resulting fine solid is filtered and then washed with 1000 ml hexane to obtain of the pure title compound 6b (304.6 gm, 0.437 mole, yield 95%).

[0048] 7-O-[2-(Chloroacetyl)]-13-[(4S,5R)-2-p-methoxyphenyl-4phenyl-3-(2-phenyl trimethylsilyl-)ethoxycarbonyl]-1,3-oxazolidinyl-5-carbonyl]baccatin III (7a)

[0049] A mixture of 7-O-(2-chloroacetyl)baccatin III (6c, 100 gm, 0.15 mole), (4S,5R) -2

methoxyphenyl-3-[(2-phenyl-2-trimethylsilyl)ethoxycarbonyl]-4-phenyl-1, oxazolidine-5-carboxylic acid (1a, 83 gm, 0.16 mole) and 4-dimethylaminopyridine (

gm, 40.9 mmol) is dissolved in toluene (0.8 L) under nitrogen atmosphere. T

temperature of the reaction mixture is raised to 50° C. under stirring and then a solution DCC (45 gm, 0.22 mole) in toluene (0.2 L) is added to it. Exotherm occurs and t

temperature of the reaction mixture automatically rises to 60° C. and that temperature maintained for 30 minutes. The reaction mixture is then cooled to 25-30° C., diluted wi

ethyl acetate (2.5 L) and kept under stirring for 15 minutes. The reaction mixture is th

filtered under suction. The residue is extracted with ethyl acetate (2×1.0 L). T

combined organic layer is washed successively with 25% ammonium chloride solution, % aqueous sodium bicarbonate, water, and brine and then dried over anhydrous sodiu

sulfate. Evaporation of the organic layer under reduced pressure affords the crude product, which is then precipitated with DCM/Hexane (1:10) to obtain compound 7a (164 gm, 0.14 mole, 93.3%).

[0050] 7,10-Di-O-[2-(Chloroacetyl)-13-[(4S,5R)-2-p-methoxyphenyl-4phenyl-3-(2-phenyl-2-trimethylsilyl)ethoxycarbonyl]-1,3-oxazolidinyl-5carbonyl]-10-deacetylbaccatin III (7b)

[0051] The compound 7b is obtained from 7,10-di-O-(2-chloroacetyl)-10-deacetylbaccatin III (6b, 110 gm, 0.158 mole), (4S,5R)-2-p-methoxyphenyl-3-[(2-phenyl-2-trimethylsilyl)ethoxycarbonyl]-4-phenyl-1,3-oxazolidine-5-carboxylic acid (1a, 88.6 gm, 0.17 mole) and 4-dimethylaminopyridine (5.27 gm, 43.1 mmol) and DCC (47.8 gm, 0.23 mole) in toluene (1.1 L) by following the protocol described above for the compound 7a.

[0052] Yield: 178 gm, 0.148 mole, 94%).

[0053] 7-O-[2-(Chloroacetyl)]-13-[(4S,5R)-2-p-methoxyphenyl-4-phenyl-3-(2-trimethylsilyl)ethoxy-carbonyl]-1,3-oxazolidinyl-5-carbonyl)]baccatin III (7c)

[0054] The compound 7c is obtained from 7-O-(2-chloroacetyl) baccatin III (6c, 100 gm, 0.15 mole), (4S,5R)-2-p-methoxyphenyl-4-phenyl-3-[(2-trimethylsilyl)ethoxycarbonyl]-1,3-oxazolidine-5-carboxylic acid (1b, 71 gm, 0.16 mole) and 4-dimethylaminopyridine (5.0 gm, 40.93 mole) and DCC (45 gm, 0.22 mole) in toluene (1.0 L) by following the protocol described above for the compound 7a.

[0055] Yield: 155 gm, 0.14 mole, 94.4%.

[0056] 7,10-Di-O-[2(Chloroacetyl)]-13-[(4S,5R)2-p-methoxyphenyl-4-phenyl-3-(2-trimethylsilyl)-ethoxycarbonyl]-5-oxazolidinyl carbonyl]-10-decaetylbaccatin III (7b)

[0057] The compound 7d is obtained from 7,10-di-O-(2-chloroacetyl)-10-deacetylbaccatin III (6b, 100 gm, 0.14 mole), (4S,5R)-2-p-methoxyphenyl-4-phenyl-3-[(2-trimethylsilyl)ethoxycarbonyl]-1,3-oxazolidine-5-carboxylic acid (1b, 66.2 gm, 0.

mole) and 4-dimethylaminopyridine (4.67 gm, 38.2 mmol) and DCC (42.4 gm, 0.

mole) in toluene (1.0 L) by following the protocol described above for the compound 7.

[0058] Yield: 149.5 gm, 0.133 mole, 95%.

[0059] 7-Chloroacetyl-13-[(4S,5R)-2,2′-dimethyl-4-phenyl-3-(trimethylsilyl)ethoxyarbonyl]-1,3-oxazolidinyl-5-carbonyl]baccatin III (7e)

[0060] The compound 7c is obtained from 7-O-(2-chloroacetyl)baccatin III (6c, 100 gm, 0.

mole), (4S,5R)-2,2-dimethyl-]-4-phenyl-3-[(2-trimethylsilyl)ethoxycarbonyl-1, oxazolidine-5-carboxylic acid (1d, 58.5 gm, 0.16 mole) and dimethylaminopyridine (5.0 gm, 40.93 mmol) and DCC (45 gm, 0.22 mole) in toluene (1 L) by following the protocol described above for the compound 7a.

[0061] Yield: 144 gm, 0.14 mole, 94.5%.

[0062] 7,10-Dichloroacetyl-13-[(4S,5R)2,2′-dimethyl-4-phenyl-3-[2-(trimethylsilyl)ethoxycarbonyl]-1,3oxazolidinyl-5carbonyl]-10-baccatin III (7f)

[0063] The compound 7f is obtained from 7,10-O-di-(2-chloroacetyl)baccatin III (6b, 100 gm, 0.14 mole), (4S,5R)-2,2-dimethyl-]-4-phenyl-3-[(2-trimethylsilyl)ethoxycarbonyl-1,3-oxazolidine-5-carboxylic acid (1d, 54.8 gm, 0.15 mole) and 4-dimethylaminopyridine (4.68 gm, 38.3 mmol) and DCC (42.4 gm, 0.205 mole) in toluene (1.0 L) by following the protocol described above for the compound 7a.

[0064] Yield: 136gm, 0.13 mole, 92.8%.

[0065] 7-O-(2Chlroacetyl)paclitaxel (9a)

[0066] 7-O-[2-(Chloroacetyl)]-13-[(4S,5R)-2-p-methoxyphenyl-4-phenyl-3-(2-phenyl-2-trimethylsilyl)-ethoxycarbonyl]-1,3-oxazolidinyl-5-carbonyl]baccatin III (7a, 116.4 gm, 0.1 mole) is suspended in dichloromethane(1.17 L) at 25-30° C. To the stirred solution is added 2 equivalents of tetrabutylammonium fluoride trihydrate (63.1 gm, 0.2 mole). Stirring is continued for 30 minutes at 25° C. and then 5% aqueous sodium bicarbonate (11.8 gm, 0.14 mole, 236 ml) is added. The reaction mixture is cooled to 0-5° C. and a solution of benzoyl chloride (17.4 ml, 0.149 mole) in dichloromethane (350

added at the same temperature over a period of 20 minutes. After the addition is stirring is continued for 15 minutes. The organic layer is separated, washed with

and dried over anhydrous sodium sulfate. The solvent is evaporated under re

pressure and the residue is subjected to column chromatography (e

ethylacetate/hexane, 2/5, v/v) to obtain the title compound 9a (77 gm, 0.083 mole, 83

[0067] Alternative method: 7-O-[2-(Chloroacetyl)]-13-[(4S,5R)-2-p-methoxyphe

phenyl-3-(2-trimethylsilyl)ethoxycarbonyl]-1,3-oxazolidinyl-5-carbonyl]baccatin

(7c, 110 gm, 0.1 mol) is suspended in 60% aquoeous trifluoroacetic acid (1.1 L, 10

and then stirred at 18-22° C. for 4.5 h, when TLC indicates completion of the rea

The reaction mixture is then diluted with dichloromethane and poured into a soluti

sodium hydrogen phosphate (2.5 Kg) in water (5.0 L) under stirring. The organic la

cooled to 0-5° C. and then a precooled solution of 5% aqueous sodium bicarbonate gm, 0.14 mole, 236 ml) is added under stirring. A solution of benzoyl chloride (17

0.149 mole) in dichloromethane (350 ml) is added slowly over a period of 20 minu

the above reaction mixture at the same temperature. After the addition is over, stirr

continued for 15 minutes. The organic layer is then separated, washed with brine dried over anhydrous sodium sulfate. The solvent is evaporated under reduced pre

and the residue is subjected to column chromatography (eluent: ethyl acetate/hexane

v/v) to obtain the title compound 9a (74.5 gm, 0.08 mole, 80%).

[0068] Alternative method: 7-Chloroacetyl-13-[(4S,5R)-2,2′-dimethyl-4-phenyl

(trimethylsilyl)ethoxyarbonyl]-1,3-oxazolidinyl-5-carbonyl]baccatin III (7e, 101 g

mole) is dissolved in 1.0 L of 60% aqueous TFA-water and the mixture is stirred 22° C. temperature for 4 h. After completion of reaction the reaction mixture is d

with dichloromethane (2.0 L) and then poured into a solution of dis

hydrogenphosphate (2.5 Kg) in water (5.0) under stirring. The dichloromethane layer separated and sodium bicarbonate (11.8 g 0.14 mole in 1000 ml of water) was added the mixture, cooled to 0-2° C. and then benzoyl chloride (17.4 ml, 0.149 mole) dissolv

in dichloromethane (350 ml) is added dropwise thereto. After addition the reacti

mixture is stirred at 28-32° C. for 2 h. The organic layer is separated and washed wi

brine and then dried over anhydrous sodium sulfate. The solvent is evaporated und

reduced pressure and the residue is subjected to column chromatography (elue

ethylacetate/hexane, 2/5, v/v) to obtain the title compound 9a (75.0 gm, 0.08 mole, 80%

as a white solid.

[0069] 7,10-Di-O-(2-chlroacetyl)docetaxel (9b)

[0070] 7,10-Di-O-[2-(Chloroacetyl)]-13-[(4S,5R)-2-p-methoxyphenyl-4-phenyl-3-(2-pheny

2-trimethylsilyl)ethoxycarbonyl]-1 3-oxazolidinyl-5-carbonyl]-10-deacetylbaccatin

(7b, 120 gm, 0.1 mole) is suspended in dichloromethane (1.2 L) at 25-30° C. To t

stirred reaction mixture is added 4 equivalents of tetrabutylammonium fluoride trihydra

(126.21 gm, 0.4 mole). Stirring is continued for 30 minutes at 25° C. and the reaction monitored by TLC. After the reaction is over dichloromethane is evaporated und

reduced pressure. The residue is taken in toluene (2.0 L) and stirred at 25-30° C. To t

stirred solution is added sodium bicarbonate (11.8 gm), followed by ditertbu

dicarbonate (30.55 gm, 0.14 mole) under stirring. The reaction mixture is stirred f

further 3 h and then sodium bicarbonate is removed by filtration. The organic layer evaporated under reduced pressure at 35-40° C. The residue is taken in ethyl acetate (2

L), washed with brine and dried over anhydrous sodium sulfate. Evaporation of t

organic layer under reduced pressure affords the compound 9b (78.8 gm, 0.082 mo

82%).

[0071] Alternative Procedure: 7,10-Di-O-[2-(Chloroacetyl)]-13-[(4S,5R)-2-methoxyphenyl-4-phenyl-3-(2-trimethylsilyl)ethoxycarbonyl]-5-oxazolidinyl carbonyl] 10-decaetylbaccatin III (7d, 112 gm, 0.099 mole) is suspended in 60% aqueo

trifluoroacetic acid (1.12 L, 10 times) and then stirred at 18-22° C. for 4.5 h, when TLC indicates completion of the reaction. The reaction mixture is then diluted with dichloromethane (2.0 L) and poured into a solution of sodium hydrogen phosphate (2.

Kg) in water (5.0 L). The organic layer is separated, washed with water, brine and dried over anhydrous sodium sulfate. Evaporation of the organic layer affords th

corresponding free amine 8b. The latter is taken in tetrahydrofuran (2.0 L) and the sodium bicarbonate (11.6 gm, 0.138 mole) followed by di-tert-butyl dicarbona

(30.55 gm, 0.14 mole) is added under stirring. After the addition is over, stirring

continued for 3 h and then sodium bicarbonate is removed by filtration. The organic laye

is evaporated under reduced pressure at 35-40° C. The residue is taken in ethyl aceta

(2.5 L), washed with brine and dried over anhydrous sodium sulfate. Evaporation of th

organic layer under reduced pressure affords the compound 9b (76 gm, 0.079 mol

79%).

[0072] Paclitaxel (10a)

[0073] To a precooled solution (0-5° C.) of 25% ammonia (150 ml) in pyridine (750 ml) is add

7-O-(2-chloroacetyl)paclitaxel (9a, 75 gm, 80.6 mmol) and then stirred at this temperatu

for 12 h. The reaction is monitored by TLC. After the reaction is over, ammonia an

pyridine is removed under low pressure. The resultant gum is dissolved in ethyl aceta

(1.5 L). The organic layer is washed successively with 2% hydrochloric acid, 5% sodiu

bicarbonate solution, and brine and then stored over anhydrous sodium sulfa

Evaporation of the organic layer under reduced pressure affords crude paclitaxel. T

latter is on column chromatography on silica 60 with ethyl acetate/hexane (6/4) affor

paclitaxel (57.8 gm, 67.69 mmol, 84%) as a white solid.

[0074] Docetaxel (10b)

[0075] Docetaxel is obtained from 7,10-O-(2-chloroacetyl)docetaxel (9b, 75 gm, 0.078 mo

using 25% ammonia (300 ml) in pyridine (1500 ml) and by following the proto

described above for paclitaxel. After column chromatography on silica 60 with eth

acetate/hexane (6/4) docetaxel is obtained as a white solid. Yield: 50.5 gm, 0.0625 mo

80.1%. 

We claim:
 1. A process for preparation of taxanes comprising subjecting 7,10-diprotected intermediates 7-O-(2-haloacyl) baccatin III 6c or 7,10-O-di-(2-haloacyl)-10-deacetylbaccatin III 6b to a step of coupling with (4S,5R)-3-[(2-alkyl/aryl-2-trialkylsilyl) ethoxy-carbonyl]-4-aryl-2-substituted-1,3-oxazolidine-5-carboxylic acid 1 in the presence of a condensation agent, an activating agent and an aromatic hydrocarbon to obtain 7-O-[2-(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3(2-unsubstituted/substituted-2-trialkylsilyl)-ethoxycarbonyl-1,3-oxazolidinyl-5-carbonyl]baccatin III 7a or 7,10-di-O[2-(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3-(2-unsubstituted/substituted-2-trialkylsily l)ethoxy-carbonyl-1,3-oxazolidinyl-5-carbonyl]-10-deacetylbaccatin III 7b; treating the coupled products 7-O-[2-(haloacyl)]-13-[(4S,5R)4-aryl-2-substituted-3-(2-substituted-2-trialkylsilyl)ethoxy-carbonyl-1,3-oxazolidinyl-5-carbonyl]baccatin III 7a or 7,10-di-O-[2(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3-(2-substituted-2-trialkylsilyl)ethoxycarbonyl-1,3-oxazolidinyl-5-carbonyl]-10-deacetylbaccatin III 7b with tetraalkylammonium halide in a haloalkane to obtain free amine of structure 8; treating free amine 8 with acid chloride or acid anhydride in the presence of a base in a heterogeneous phase to obtain the intermediates of structure 9; subjecting the intermediates of compound 9 to the deprotection of 2-haloacyl group under mild alkaline condition at −20 to +40° C. for 6-24 h in the presence of ammonia or aliphatic amines or aromatic amines or their combination to obtain paclitaxel or docetaxel.
 2. A process for the preparation of coupled product 7 comprising subjecting 7,10-diprotected intermediates 7-O-(2-haloacyl) baccatin III 6c or 7,10-O-di-(2-haloacyl)10-deacetylbaccatin III 6b to a step of coupling with (4S,5R)-3-[(2-alkyl/aryl-2-trialkylsilyl) ethoxy-carbonyl]4-phenyl-2-substituted-1,3-oxazolidine-5-carboxylic acid 1 in the presence of a condensation agent, an activating agent and an aromatic hydrocarbon to obtain 7-O-[2-(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3(2-unsubstituted/substituted-2-trialkylsilyl)-ethoxycarbonyl-1,3-oxazolidinyl-5-carbonyl]baccatin III 7a or 7,10-di-O[2-(haloacyl)]-13-[(4S,5R)-4-aryl-2-substituted-3-(2-unsubstituted/substituted-2-trialkylsilyl)ethoxy-carbonyl-1,3-oxazoli-dinyl-5-carbonyl]-10-deacetylbaccatin III 7b.
 3. A process as claimed in claim 1 wherein said condensation agent is preferably dicyclohexylcarbodiimide and the activating agent is preferably am inopyridine most preferably 4-dimethyl-aminopyridine.
 4. A process as claimed in claim 1 wherein said aromatic hydrocarbon is preferably toluene.
 5. A process as claimed in claim 1 wherein the coupling reaction is carried out at a temperature between 0-100° C. and preferably at 40-80° C., most preferably at 60° C.
 6. A process as claimed in claim 1 wherein said tetraalkylammonium halide is tetrabutylammonium fluoride.
 7. A process as claimed in claim 1 wherein tetrabutylammonium fluoride in haloalkane, preferably dichloromethane is used.
 8. A process as claimed in claim 1 wherein deprotection of haloacyl group in the intermediate of compound 9 is carried out by treating compound 9 with 2:10 ammonia and pyridine preferably at 0-5° C., most preferably at 2° C. for 6-24 h, preferably for 10 h.
 9. A process for the preparation of oxazolidine carboxylic acid, of formula 1 comprising condensing phenylisoserine with a (2-trialkylsilyl)ethyl haloformate in the presence of a base to obtain a N-protected isoserine, followed by converting the same into the corresponding methyl ester, treating the said ester with an alkoxyalkane or aryloxyalkane in the presence of a catalytic amount of arylsulfonic acid to obtain 5-oxazolidine carboxylic acid esters and hydrolysing the said esters in the presence of an alkali.
 10. The intermediate compound of formula
 7. 11. The compound 7a as claimed in claim 10 wherein the compound is 7-O-[2-(chloroacetyl)]-13-[(4S,5R) -2-p-methoxyphenyl-4-phenyl-3-(2-phenyl-2-trimethylsilyl-) ethoxycarbonyl]-1,3-oxazolidinyl-5-carbonyl]baccatin III.
 12. The compound 7b as claimed in claim 10 wherein the compound is 7,10-di-O-[2-(chloroacetyl)]-13-[(4S,5R)-2-p-methoxyphenyl-4-phenyl-3-(2-phenyl-2-trimethylsilyl)-ethoxycarbonyl]-1,3-oxazolidinyl-5-carbonyl]-10-deacetyl baccatin III.
 13. The compound 7c as claimed in claim 10 wherein the compound is 7-O-[2-chloroacetyl)]-13-[(4S,5R)-2-p-methoxyphenyl-4-phenyl-3-(2-trimethylsilyl)-ethoxycarbonyl]-1,3-oxazolidinyl-5-carbonyl]baccatin
 111. 14. The compound 7 d as claimed in claim 10 wherein the compound is 7,10-di-O-[2-(chloroacetyl)]-13-[(4S,5R)-2-p-methoxyphenyl4-phenyl-3-(2-trimethylsilyl)ethoxycarbonyl-5-oxazolidinyl carbonyl]-1-deacetylbaccatin III.
 15. The oxazolidine carboxylic acid of formula
 1. 16. The compound of formula
 8. 17. The compound of formula
 9. 